SCHEMBL4422850

SCHEMBL4422850

CCCC(C[C@H]1[C@H](O)[C@@H](OC(=O)O)C[C@H]1N)C(C)CNC(C)=O

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL4413595 1.00 — —
SCHEMBL4411243 0.93 — —
SCHEMBL4417831 0.85 — —
SCHEMBL7231029 0.84 NEU2 (0.34) —
SCHEMBL4416900 0.75 — —
SCHEMBL7231650 0.71 NEU2 (0.32) —
SCHEMBL4423891 0.70 NEU2 (0.33) —
SCHEMBL4419137 0.67 — —
SCHEMBL4417976 0.65 NEU2 (0.50) —
SCHEMBL4415941 0.65 NEU2 (0.50) —

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1040094-B9 SUBSTITUTED CYCLOPENTANE AND CYCLOPENTENE COMPOUNDS USEFUL AS NEURAMINIDASE INHIBITORS BIOCRYST PHARM INC (US) 2015-09-09 — — EP claimed
EP-1040094-B1 SUBSTITUTED CYCLOPENTANE AND CYCLOPENTENE COMPOUNDS USEFUL AS NEURAMINIDASE INHIBITORS BIOCRYST PHARM INC (US) 2009-03-18 — — EP claimed
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